Periodontal Probe Number 18 Handle Number 30 Qulix 3-5-8-10 - Hu-Friedy - Delynov
The Sonde parodontale #18 manche #30 Qulix 3-5-8-10 - Hu-Friedy is a medical device manufactured by Hu-Friedy Mfg. Co., LLC.
- Compliance: Medical device Class I.
- Manufacturer: Hu-Friedy Mfg. Co., LLC.
- Reserved for healthcare professionals. Read instructions carefully before use.
What is the #18 periodontal probe #30 handle Qulix 3-5-8-10?
The #18 periodontal probe #30 handle Qulix 3-5-8-10 is a manual diagnostic instrument designed by the manufacturer Hu-Friedy. This tool consists of a thin, calibrated working part mounted on a #30 type handle. Qulix technology uses black color markings that do not fade easily, facilitating visibility during clinical examination. This 18 periodontal probe is specifically calibrated to offer clear visual cues to practitioners when evaluating biological space and the health of the tooth's supporting tissues.
What are the clinical indications for this instrument?
In oral surgery and periodontology, this instrument is indicated for performing a complete periodontal assessment. It is primarily used for periodontal pocket measurement to evaluate the severity of periodontitis or gingivitis. The 3-5-8-10 periodontal probe also allows for measuring gingival recession, evaluating the clinical attachment level, and checking for bleeding on probing. It is used systematically during initial examinations, post-treatment re-evaluations, and maintenance visits to monitor the evolution of periodontal tissues around natural teeth.
What are the technical characteristics of the Hu-Friedy probe?
This 3-5-8-10 periodontal probe is distinguished by its Qulix graduation system at intervals of 3mm, 5mm, 8mm, and 10mm. These precise markings allow for direct and unambiguous reading of the sulcus or pocket depth. The #30 handle offers a grip adapted to the requirements of daily practice. Manufactured by Hu-Friedy Mfg. Co., LLC, this periodontal exploration probe benefits from a rigorous design to ensure the thinness of the working tip, thereby limiting patient discomfort while maintaining sufficient rigidity for optimal tactile transmission of subgingival contours.
What are the contraindications for the use of this device?
According to information provided by the manufacturer Hu-Friedy, there are no specific medical contraindications listed for the use of this diagnostic instrument, outside of standard protocols related to the patient's general health status. However, use of the probe should be avoided on extremely inflammatory or fragile tissues without controlled pressure to avoid distorting measurements or causing unnecessary trauma. Like any metallic instrument, its use should be evaluated in patients with extreme sensitivities to alloy components, although this is rare for non-permanent diagnostic instruments.
What are the maintenance and durability precautions?
The #18 periodontal probe is a non-resorbable and reusable instrument that requires sterilization between each patient. As a Class I device, it must be processed according to the decontamination, cleaning, and autoclave sterilization protocols in force in dental practices. It is recommended to read the instructions carefully before use to comply with the cleaning cycles recommended by Hu-Friedy. Particular attention should be paid to the integrity of the Qulix 3-5-8-10 markings to ensure the accuracy of clinical measurements over the long term. Any blunt or bent instrument must be replaced to maintain diagnostic reliability.
Who is the manufacturer and what standards are respected?
The official manufacturer of this medical device is Hu-Friedy Mfg. Co., LLC, located in Chicago, USA. This product is classified as a Class I medical device according to current regulations. Compliance with manufacturing standards by Hu-Friedy ensures health professionals an instrument that meets safety and performance requirements for the intended use in dental surgery. As a Class I product, it is reserved exclusively for duly trained health professionals. The absence of specific CE marking in the source data implies that the practitioner must refer to the technical manual and local directives to validate compliance for use in their geographic area.
State of the art
Specialized surgical instrumentation is evolving towards ergonomic designs.
Specifications
| Manufacturer | Hu-Friedy |
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